Pure Global

Ventricular prosthesis system - UK MHRA Medical Device Registration

Ventricular prosthesis system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 134519. The device is manufactured by SynCardia Systems, LLC from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Emergo Consulting (UK) Limited .

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
MHRA Registered
Active implantable device (Directive 90/385/EEC only)
๐Ÿ‡ฌ๐Ÿ‡ง
Ventricular prosthesis system
MHRA Device ID: 134519

Device Type

Active implantable device (Directive 90/385/EEC only)

Devices

Ventricular prosthesis system

Type

Active implantable Medical device

Date Registered

Jan 31, 2022

Last Updated

Dec 22, 2022

Manufacturer Information

Address

1992 East Silverlake Road

Tucson, Arizona, United States

Created Date

Jan 31, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 โ€“ UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (10)

Soft-tissue/mesh anchor, non-bioabsorbable

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Noninvasive device battery charger

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connection

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system external electrode

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system programmer

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, extracorporeal

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Personal device holder, reusable

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Neurosurgical procedure kit, non-medicated, single-use

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Implantable sleep apnoea treatment system programmer/charger

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Nyxoah SA

Implantable sleep apnoea treatment system, fixed-rate

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Nyxoah SA